4-Chloro-1-propyl[1,2,4]triazolo[4,3-a]quinoxaline → 1-Butyl-N-cyclopentyl[1,2,4]triazolo[4,3-a]quinoxalin-4-amine

HRID 868518

Reaction equation

HRID 868518 reaction equation
Cl[C:2]1[C:3]2[N:4]([C:12]([CH2:15][CH2:16][CH2:17][CH3:18])=[N:13][N:14]=2)[C:5]2[C:10]([N:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2.ClC1C2N(C(CCC)=NN=2)[C:23]2[C:28]([N:29]=1)=[CH:27][CH:26]=[CH:25]C=2>>[CH2:15]([C:12]1[N:4]2[C:5]3[C:10]([N:11]=[C:2]([NH:29][CH:28]4[CH2:27][CH2:26][CH2:25][CH2:23]4)[C:3]2=[N:14][N:13]=1)=[CH:9][CH:8]=[CH:7][CH:6]=3)[CH2:16][CH2:17][CH3:18]

Participants

3

Reactant 2

HCID 133857074-Chloro-1-propyl[1,2,4]triazolo[4,3-a]quinoxalineHCID 142806084-Chloro-1-butyl[1,2,4]triazolo[4,3-a]quinoxaline

Product 1

HCID 142806121-Butyl-N-cyclopentyl[1,2,4]triazolo[4,3-a]quinoxalin-4-amine

Procedure

The title compound was prepared essentially as described in Example 4 substituting 4-chloro-1-butyl[1,2,4]triazolo[4,3-a]quinoxaline for 4-chloro-1-propyl[1,2,4]triazolo[4,3-a]quinoxaline; mp 195°-197° C.

Sources & evidence

ORD record
ord-cdc859f1dfd4455e8872df1e8116a2ec
Source dataset
uspto-grants-1988_10
Patent number
US04780464

Linked notes

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